NCT02123810

Brief Summary

The investigators sought to evaluate the influence of fatigue after a night shift on the quality of Chest Compressions (CC) in CardioPulmonary Resuscitation (CPR), among physicians.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
46

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2014

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2014

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

April 22, 2014

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 28, 2014

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2014

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2014

Completed
Last Updated

July 22, 2015

Status Verified

July 1, 2015

Enrollment Period

5 months

First QC Date

April 22, 2014

Last Update Submit

July 20, 2015

Conditions

Cardiac Arrest

Keywords

fatiguemotor skillscardiopulmonary resuscitation

Outcome Measures

Primary Outcomes (1)

  • the proportion of CC with a depth higher than 50mm

    The investigators evaluated the quality of CC with a low-fidelity manikin and its electronic feedback device.

    2 minutes of chest compressions

Secondary Outcomes (1)

  • Number of chest compressions

    2 minutes

Other Outcomes (1)

  • Factors associated with better chest compressions (CC)

    2 minutes

Study Arms (2)

Control

OTHER

The investigators measure quality of chest compressions before nightshift. Control group

Other: CPR

OFF

OTHER

The investigators measure quality of chest compressions before nightshift. After night shift group

Other: CPR

Interventions

CPROTHER

Simulated cardiac arrest on a manikin Chest Compression CPR for 6 minutes

ControlOFF

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Resident / Physicians in emergency departement (ED) or taking night in ED
  • Resident / Physicians in Intensive Care Unit (ICU) or taking night in ED
  • Nightshift \> 18 hours

You may not qualify if:

  • Stop chest compressions before 2 minutes

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hôpital Pitié-Salpêtrière; Hopital Saint Antoine; Hopital Tenon

Paris, France

Location

MeSH Terms

Conditions

Heart ArrestFatigue

Interventions

Cardiopulmonary Resuscitation

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

ResuscitationEmergency TreatmentTherapeutics

Study Officials

  • Yonathan Freund

    Emergency Department, Hôpital Pitié-Salpêtrière, 47-83 Boulevard de l'Hôpital, 75013 Paris, France.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor

Study Record Dates

First Submitted

April 22, 2014

First Posted

April 28, 2014

Study Start

April 1, 2014

Primary Completion

September 1, 2014

Study Completion

October 1, 2014

Last Updated

July 22, 2015

Record last verified: 2015-07

Locations

FR(1)